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FDA Warning Letter: Major CGMP Violations in Drug Manufacturing and Quality Systems This FDA warning letter identifies significant violations of Current Good Manufacturing Practice (CGMP) requirements at a foreign drug manufacturing facility registered with the U.S. Food and Drug Administration (FDA) as a manufacturer of over-the-counter (OTC) drug products. The FDA warning letter was issued … Read more
FDA Warning Letter: Major CGMP, Quality System and OTC Drug Violations This FDA warning letter identifies significant violations of Current Good Manufacturing Practice (CGMP) requirements for finished pharmaceuticals under 21 CFR Parts 210 and 211. FDA concluded that the firm’s manufacturing, processing, packing, and holding controls did not conform to CGMP requirements, resulting in drug … Read more
FDA Warning Letter An FDA warning letter is a serious regulatory communication that identifies significant violations of FDA requirements and allows a pharmaceutical manufacturer to take corrective action. In this case, the FDA warning letter identifies three major CGMP deficiencies related to finished-product testing, incoming material controls, and cleaning validation. These findings demonstrate the importance … Read more